ENST00000614878.4 ANKRD13B
Information
- Transcript ID
- ENST00000614878.4
- Genome
- hg38
- Position
- chr17:29,593,468-29,614,760
- Strand
- +
- CDS length
- 1,881
- Amino acid length
- 627
- Gene symbol
- ANKRD13B
- Gene type
- protein-coding
- Gene description
- ankyrin repeat domain 13B
- Gene Entrez Gene ID
- 124930
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
Exon
| Exon number | Start | Stop |
|---|---|---|
| 1 | 29,593,468 | 29,593,735 |
| 2 | 29,607,742 | 29,607,877 |
| 3 | 29,607,986 | 29,608,110 |
| 4 | 29,608,195 | 29,608,240 |
| 5 | 29,608,851 | 29,608,994 |
| 6 | 29,609,086 | 29,609,275 |
| 7 | 29,609,355 | 29,609,421 |
| 8 | 29,610,685 | 29,610,766 |
| 9 | 29,611,579 | 29,611,643 |
| 10 | 29,611,876 | 29,612,006 |
| 11 | 29,612,116 | 29,612,273 |
| 12 | 29,612,402 | 29,612,554 |
| 13 | 29,612,652 | 29,612,815 |
| 14 | 29,612,887 | 29,612,963 |
| 15 | 29,613,354 | 29,613,719 |
| 16 | 29,614,263 | 29,614,760 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 29,593,622 | 29,593,735 |
| 2 | CDS | 29,607,742 | 29,607,877 |
| 3 | CDS | 29,607,986 | 29,608,110 |
| 4 | CDS | 29,608,195 | 29,608,240 |
| 5 | CDS | 29,608,851 | 29,608,994 |
| 6 | CDS | 29,609,086 | 29,609,275 |
| 7 | CDS | 29,609,355 | 29,609,421 |
| 8 | CDS | 29,610,685 | 29,610,766 |
| 9 | CDS | 29,611,579 | 29,611,643 |
| 10 | CDS | 29,611,876 | 29,612,006 |
| 11 | CDS | 29,612,116 | 29,612,273 |
| 12 | CDS | 29,612,402 | 29,612,554 |
| 13 | CDS | 29,612,652 | 29,612,815 |
| 14 | CDS | 29,612,887 | 29,612,963 |
| 15 | CDS | 29,613,354 | 29,613,582 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr17 | 27,920,486 | 27,941,778 | Link |
CDS sequence
ATGATCCCCGCCAACGCCTCCGCCAGGAAGGGGCCCGAGGGCAAGTATCCGCTGCACTACCTCGTGTGGCACAACCGCCACCGCGAGCTGGAGAAGGAGGTCCGCGCGGGCCAGGTGGACATCGAGCAGCTGGATCCCCGCGGCCGGACTCCCCTGCACCTGGCCACCACGCTGGGGCACCTTGAGTGTGCCCGTGTGCTCCTGGCGCACGGCGCAGACGTGGGCAGGGAGAATCGCAGCGGCTGGACAGTGCTCCAGGAGGCTGTGAGTACCCGGGACCTGGAGCTGGTGCAGCTGGTGCTTCGGTACCGGGACTACCAGCGGGTGGTGAAGCGGCTGGCGGGCATCCCCGTGCTCCTGGAGAAGCTGCGCAAGGCCCAGGACTTCTACGTGGAGATGAAATGGGAGTTCACTAGCTGGGTGCCCCTGGTGTCCAAGATCTGCCCTAGTGACACCTACAAAGTGTGGAAGAGCGGCCAGAACCTGAGGGTAGACACCACACTCCTGGGCTTTGACCACATGACCTGGCAGCGAGGGAACCGCAGCTTTGTCTTCAGGGGCCAAGACACAAGCGCCGTGGTCATGGAGATTGACCACGACCGCCGGGTGGTGTACACAGAGACTCTGGCACTGGCTGGGCAGGACCGGGAGCTGCTGCTGGCTGCTGCTCAGCCCACTGAGGAACAGGTGCTGAGCCGGCTTACCGCGCCCGTCGTCACCACTCAGCTTGACACCAAGAATATCTCCTTTGAGAGGAACAAGACTGGCATCCTGGGCTGGCGCAGTGAAAAGACGGAGATGGTGAATGGGTATGAAGCTAAGGTGTATGGGGCATCTAACGTGGAGCTCATCACCCGCACACGGACAGAACATCTTTCAGAACAGCACAAGGGCAAGGTCAAAGGCTGTAAGACACCTTTGCAGTCCTTCCTGGGAATCGCTGAGCAGCACGGGGGCCCCCAAAATGGGACCCTGATCACTCAGACTCTGAGCCAAGCCAACCCCACTGCCATCACTGCAGAAGAATACTTCAACCCCAACTTTGAGCTGGGCAACCGTGATATGGGCCGCCCCATGGAACTGACCACCAAGACACAGAAGTTCAAGGCCAAGCTGTGGCTGTGTGAGGAGCATCCCCTGTCCCTGTGTGAGCAGGTGGCCCCCATCATTGACCTCATGGCCGTCAGCAATGCGCTTTTTGCCAAGCTCCGGGACTTCATCACCCTGCGTCTGCCTCCTGGCTTCCCAGTTAAGATTGAAATCCCGATCTTCCACATCCTCAACGCCCGCATCACCTTCGGGAACCTCAACGGCTGCGACGAACCGGTGCCATCGGTGCGAGGCAGCCCCAGCAGCGAGACGCCTTCCCCAGGCAGCGACTCCTCCAGCGTCAGCAGCTCCAGCTCCACGACCTCCTGCCGCGGCTGCGAGATCTCCCCAGCGTTGTTCGAGGCCCCGCGCGGCTACAGCATGATGGGCGGCCAGCGGGAGGCGGCGACCCGGGACGACGACGACGACCTGCTGCAATTCGCCATCCAGCAGAGCCTGCTTGAGGCGGGCAGTGAGTATGACCAGGTCACCATCTGGGAGGCGCTAACCAACAGCAAGCCAGGCACCCACCCCATGTCCTACGAGGGTCGCCGACAGGACAGGAGCGCCCCGCCCACGCCGCAGCGCCAGCCTGCGCCCCCGGCGTCAGTGCCCAGCCCTCGGCCCAGCTCAGGGCCAGGTTCCGGCGGCCACGTGTTCCGGAGCTACGACGAGCAGCTGCGGCTGGCGATGGAACTGTCGGCGCAGGAGCAGGAGGAGAGGCGGCGGCGCGCGCGCCAGGAGGAGGAGGAGCTGGAGCGCATCCTGAGGCTCTCACTGACCGAGCAGTAG
Amino sequence
MIPANASARKGPEGKYPLHYLVWHNRHRELEKEVRAGQVDIEQLDPRGRTPLHLATTLGHLECARVLLAHGADVGRENRSGWTVLQEAVSTRDLELVQLVLRYRDYQRVVKRLAGIPVLLEKLRKAQDFYVEMKWEFTSWVPLVSKICPSDTYKVWKSGQNLRVDTTLLGFDHMTWQRGNRSFVFRGQDTSAVVMEIDHDRRVVYTETLALAGQDRELLLAAAQPTEEQVLSRLTAPVVTTQLDTKNISFERNKTGILGWRSEKTEMVNGYEAKVYGASNVELITRTRTEHLSEQHKGKVKGCKTPLQSFLGIAEQHGGPQNGTLITQTLSQANPTAITAEEYFNPNFELGNRDMGRPMELTTKTQKFKAKLWLCEEHPLSLCEQVAPIIDLMAVSNALFAKLRDFITLRLPPGFPVKIEIPIFHILNARITFGNLNGCDEPVPSVRGSPSSETPSPGSDSSSVSSSSSTTSCRGCEISPALFEAPRGYSMMGGQREAATRDDDDDLLQFAIQQSLLEAGSEYDQVTIWEALTNSKPGTHPMSYEGRRQDRSAPPTPQRQPAPPASVPSPRPSSGPGSGGHVFRSYDEQLRLAMELSAQEQEERRRRARQEEEELERILRLSLTEQ*